Canonical Allele Identifier: CA399220249
Gene: CCL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.35880232G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880232G>A , CM000679.2:g.35880232G>A GRCh38
NC_000017.9:g.31231349G>A NCBI36
NG_015990.1:g.5142C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000603197.6:c.74C>T ENSP00000474412.1:p.Pro25Leu
ENST00000605140.6:c.74C>T MANE Select ENSP00000475057.1:p.Pro25Leu
ENST00000605509.2:c.74C>T ENSP00000474141.2:p.Pro25Leu
ENST00000651122.1:c.74C>T ENSP00000499138.1:p.Pro25Leu
ENST00000603197.5:c.74C>T ENSP00000474412.1:p.Pro25Leu
ENST00000605140.5:c.74C>T ENSP00000475057.1:p.Pro25Leu
ENST00000605509.1:c.60C>T
NM_001278736.1:c.74C>T NP_001265665.1:p.Pro25Leu
NM_002985.2:c.74C>T NP_002976.2:p.Pro25Leu
XR_934696.1:n.197-4150G>A
XR_934697.1:n.200-4150G>A
XR_001752852.1:n.426+158G>A
XR_934696.2:n.91-4150G>A
XR_934697.2:n.91-4150G>A
NM_001278736.2:c.74C>T NP_001265665.1:p.Pro25Leu
NM_002985.3:c.74C>T MANE Select NP_002976.2:p.Pro25Leu